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多壁碳纳米管上硫化钼纳米束的工程制备:通过可控溶剂热沉积调控活性位点和电子导电性

Engineering of Molybdenum Sulfide Nanobunches on MWCNTs: Modulation of Active Sites and Electronic Conductivity via Controllable Solvothermal Deposition.

作者信息

Ali Aya, Basuni Mustafa, Shams-Eldin Reham, Pilz Lena, Hashem Tawheed, Heinle Marita, Nefedov Alexei, Amin Muhamed, Tsotsalas Manuel, Drazic Goran, Hassanien Abdou, Alkordi Mohamed H

机构信息

Center for Materials Science, Zewail City of Science and Technology, Giza 12578, Egypt.

Institute of Functional Interfaces, Karlsruhe Institute of Technology (KIT), 76344 Eggenstein-Leopoldshafen, Germany.

出版信息

ACS Appl Nano Mater. 2023 Mar 10;6(5):3627-3636. doi: 10.1021/acsanm.2c05311. Epub 2023 Feb 16.

Abstract

Amorphous, mixed-valency, molybdenum sulfide (MoS) with a proposed formula Mo Mo (S )(S), was grown through one-pot, solvothermal synthesis on multi-walled carbon nanotubes (MWCNTs) in a gram-scale setup. Optimizing the loading of the active catalyst relative to the conductive support resulted in optimized catalytic performance in hydrogen evolution reaction (HER), reaching down to one of the lowest reported overpotentials, η = 140 mV and η = 198 mV with a Tafel slope of 62 mV/dec, for the 6.5 wt% MoS@MWCNTs. Engineering this amorphous MoS catalyst was made possible through control of the oxidation state of Mo, to avoid the fully reduced MoS phases. We also demonstrate that engineering defects in the MoS catalyst does not require sophisticated techniques (e.g. UHV deposition, ion beam sputtering, pulsed laser ablation), but can rather be induced simply through controlling the reductive synthesis conditions.

摘要

通过一锅法溶剂热合成,在克级规模装置中,在多壁碳纳米管(MWCNTs)上生长出了一种非晶态、具有混合价态的硫化钼(MoS),其化学式为Mo Mo (S )(S)。相对于导电载体优化活性催化剂的负载量,使得析氢反应(HER)的催化性能得到优化,对于6.5 wt%的MoS@MWCNTs,其过电位低至已报道的最低值之一,η = 140 mV和η = 198 mV,塔菲尔斜率为62 mV/dec。通过控制Mo的氧化态来制备这种非晶态MoS催化剂成为可能,从而避免了完全还原的MoS相。我们还证明,在MoS催化剂中引入缺陷并不需要复杂的技术(例如超高真空沉积、离子束溅射、脉冲激光烧蚀),而是可以通过简单地控制还原合成条件来实现。

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All The Catalytic Active Sites of MoS for Hydrogen Evolution.所有 MoS 用于析氢反应的催化活性位。
J Am Chem Soc. 2016 Dec 28;138(51):16632-16638. doi: 10.1021/jacs.6b05940. Epub 2016 Dec 15.

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